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FDA 510(k)

DERMAGRAN WENT DRESSING (DEXTROSE-SALINE)

K-Number: K954741 · 1995-11-01

ApplicantDerma Sciences, Inc.
Decision Date1995-11-01
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

DERMAGRAN WENT DRESSING (DEXTROSE-SALINE) is the device name listed in this FDA 510(k) record. The listed applicant is Derma Sciences, Inc.. It received FDA 510(k) clearance on 1995-11-01 under 510(k) number K954741. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DERMAGRAN WENT DRESSING (DEXTROSE-SALINE)?

DERMAGRAN WENT DRESSING (DEXTROSE-SALINE) is a medical device that received FDA 510(k) clearance on 1995-11-01. The listed applicant is Derma Sciences, Inc.. The 510(k) number is K954741.

When did DERMAGRAN WENT DRESSING (DEXTROSE-SALINE) receive FDA 510(k) clearance?

DERMAGRAN WENT DRESSING (DEXTROSE-SALINE) received FDA 510(k) clearance on 1995-11-01, under 510(k) number K954741.

Who is the listed applicant for DERMAGRAN WENT DRESSING (DEXTROSE-SALINE)?

The FDA 510(k) record lists Derma Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERMAGRAN WENT DRESSING (DEXTROSE-SALINE)?

The FDA product code for DERMAGRAN WENT DRESSING (DEXTROSE-SALINE) is MGQ.

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Other records listing Derma Sciences, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K110546MEDIHONEY HYDROGEL SHEET DRESSINGS WITH ACTIVE LEPTOSPERMUM HONEYK101793MEDIHONEY GEL DRESSING WITH ACTIVE MANUKA HONEYK081584DERMA SCIENCES OTC MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEYK080315DERMA SCIENCES MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEYK072956MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEYK970660DERMAGRAN WOUND MANAGEMENT SYSTEM

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Related Devices (Code: MGQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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